Nanoparticle compositions and additive packages

Information

  • Patent Grant
  • 9650589
  • Patent Number
    9,650,589
  • Date Filed
    Thursday, September 3, 2015
    8 years ago
  • Date Issued
    Tuesday, May 16, 2017
    7 years ago
  • Inventors
  • Examiners
    • Hines; Latosha
    Agents
    • Akerman LLP
    • Glazier; Stephen C.
Abstract
Additive packages including multifunctional additive molecules are disclosed, including, for example, organic medium intercalated with lubricant nanoparticles. The additive package may be greaseless or may be added to materials such as base oils or greases, greaseless materials, or anti-corrosives, for example. The additive package added to materials may form a coating or lubricant that may be added to a surface of an object.
Description
BACKGROUND

Over the years, considerable effort has been expended to develop nanostructures that can be used as lubricants, coatings, or delivery mechanisms. New ways to improve nanoparticle compositions, their method of manufacture, and their use are sought.


SUMMARY

In one aspect, a composition is described, comprising solid lubricant nanoparticles and an organic medium.


In another aspect, nanoparticles comprising a layered material are disclosed.


In a further aspect, a method of producing a nanoparticle comprising milling layered materials is provided.


In yet another aspect, a method of making a lubricant is disclosed, in which the method comprises milling layered materials to form nanoparticles and incorporating the nanoparticles into a base to form a lubricant.


Other aspects will become apparent by consideration of the detailed description and accompanying drawings.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a diagram illustrating a method of producing solid lubricant nanoparticles.



FIG. 2 is a diagram illustrating one method of preparing nanoparticle based lubricants.



FIG. 3 shows transmission electron microscopy (TEM) micrographs of molybdenum disulfide particles. Panel (A) shows molybdenum disulfide as it is available, typically from about a few microns to submicron size. Panel (B) shows molybdenum disulfide that has been ball milled in air for 48 hours. Panel (C) is a high resolution electron microscopy image that shows molybdenum disulfide that has been ball milled in air for 48 hours. Panel (D) is a high-resolution transmission electron microscopy (HRTEM) image that shows molybdenum disulfide that has been ball milled in air for 48 hours followed by ball milling in oil for 48 hours.



FIG. 4 is a graph showing XRD spectra of molybdenum disulfide particles. Line (A) is the XRD spectra for molybdenum disulfide that has been ball milled in air for 48 hours followed by ball milling in oil for 48 hours. Line (B) is the XRD spectra for molybdenum disulfide that has been ball milled in air for 48 hours. Line (C) is the XRD spectra for molybdenum disulfide that has not been ball milled.



FIG. 5 is a graph showing XPS spectra of molybdenum disulfide particles in which the carbon peak for molybdenum disulfide that has not been ball milled is shown, as well as the carbon peak for molybdenum disulfide that has been ball milled in air for 48 hours, followed by ball milling in oil for 48 hours.



FIGS. 6(A)-6(D) show graphs and bar charts depicting tribological test data for different additives in paraffin oil. FIG. 6(A) shows the average wear scar diameter for a base oil (paraffin oil), paraffin oil with micron sized MoS2, paraffin oil with MoS2 that was milled in air for 48 hours, and paraffin oil with MoS2 that was milled in air for 48 hours followed by milling in canola oil for 48 hours. FIG. 6(B) shows the load wear index for paraffin oil without a nanoparticle additive, paraffin oil with micron sized MoS2, paraffin oil with MoS2 that was milled in air for 48 hours, and paraffin oil with MoS2 that was milled in air for 48 hours followed by milling in canola oil for 48 hours. FIG. 6(C) shows the coefficient of friction for paraffin oil without a nanoparticle additive, paraffin oil with micron sized MoS2 (c-MoS2), paraffin oil with MoS2 that was milled in air for 48 hours (d-MoS2), and paraffin oil with MoS2 that was milled in air for 48 hours followed by milling in canola oil for 48 hours (n-MoS2). FIG. 6(D) shows the extreme pressure data for paraffin oil with micron sized MoS2 (c-MoS2), paraffin oil with MoS2 that was milled in air for 48 hours (d-MoS2), and paraffin oil with MoS2 that was milled in air for 48 hours followed by milling in canola oil for 48 hours (n-MoS2); in each test the solid lubricant nanoparticle additive was present in the amount of 1% by weight.



FIG. 7 is a TEM image showing the architecture of molybdenum disulfide nanoparticles (15-70 nm average size). Panel (a) shows the close caged dense oval shaped architecture of molybdenum disulfide nanoparticles that have been ball milled in air for 48 hours. Panel (b) shows the open ended oval shaped architecture of molybdenum disulfide nanoparticles that have been ball milled in air for 48 hours followed by ball milling in canola oil for 48 hours.



FIG. 8 is a graph depicting a comparison of wear scar diameters for different additives in paraffin oil. One additive is crystalline molybdenum disulfide (c-MoS2). Another is molybdenum disulfide nanoparticles that were ball milled in air (n-MoS2). Another additive is molybdenum disulfide nanoparticles that were ball milled in air followed by ball milling in canola oil and to which a phospholipid emulsifier was added (n-MoS2+Emulsifier).



FIG. 9 shows photographs and graphs produced using energy dispersive x-ray analysis (EDS) depicting the chemical analysis of wear scar diameters in four-ball tribological testing for nanoparticle based lubricants. Panel (a) shows paraffin oil without any nanoparticle composition additive. Panel (b) shows paraffin oil with molybdenum disulfide nanoparticles that have been ball milled in air for 48 hours followed by ball milling in oil for 48 hours and treated with a phospholipid emulsifier.





DETAILED DESCRIPTION

Before any embodiments are explained in detail, it is to be understood that the invention is not limited in its application to the details of construction and the arrangement of components set forth in the following description or illustrated in the following drawings. The invention is capable of other embodiments and of being practiced or of being carried out in various ways. Also, it is to be understood that the phraseology and terminology used herein is for the purpose of description and should not be regarded as limiting.


Any numerical range recited herein includes all values from the lower value to the upper value. For example, if a concentration range is stated as 1% to 50%, it is intended that values such as 2% to 40%, 10% to 30%, or 1% to 3%, etc., are expressly enumerated in this specification. These are only examples of what is specifically intended, and all possible combinations of numerical values between and including the lowest value and the highest value enumerated are to be considered to be expressly stated in this application.


Herein described are compositions and methods for making compositions comprising solid lubricant nanoparticles and an organic medium. Also described are nanoparticles comprising layered materials. The nanoparticles may be solid lubricant nanoparticles. The nanoparticles may be made from starting materials or solid lubricant starting materials. Examples of solid lubricants may include, but are not limited to, layered materials, suitably chalcogenides, more suitably, molybdenum disulphide, tungsten disulphide, or a combination thereof. Another suitable layered material is graphite or intercalated graphite. Other solid lubricants that may be used alone or in combination with the layered materials are polytetrafluoroethylene (Teflon®), boron nitride (suitably hexagonal boron nitride), soft metals (such as silver, lead, nickel, copper), cerium fluoride, zinc oxide, silver sulfate, cadmium iodide, lead iodide, barium fluoride, tin sulfide, zinc phosphate, zinc sulfide, mica, boron nitrate, borax, fluorinated carbon, zinc phosphide, boron, or a combination thereof. Fluorinated carbons may be, without limitation, carbon-based materials such as graphite which has been fluorinated to improve its aesthetic characteristics. Such materials may include, for example, a material such as CFx wherein x ranges from about 0.05 to about 1.2. Such a material is produced by Allied Chemical under the trade name Accufluor.


The methods may include milling a solid lubricant feed. In one embodiment, the solid lubricant feed may be capable of being milled to particles comprising an average dimension of about 500 nanometers (submicron size) to about 10 nanometers. Suitably, the particles may have an average particle dimension of less than or equal to about 500 nanometers, suitably less than or equal to about 100 nanometers, suitably less than or equal to about 80 nanometers, and more suitably less than or equal to about 50 nanometers. Alternatively, the ball milling may result in milled solid lubricant particles comprising a mixture, the mixture comprising particles having an average particle dimension of less than or equal to about 500 nanometers, plus larger particles. Milling may include, among other things, ball milling and chemo mechanical milling. Examples of ball milling may include dry ball milling, wet ball milling, and combinations thereof. Ball milling may refer to an impaction process that may include two interacting objects where one object may be a ball, a rod, 4 pointed pins (jack shape), or other shapes. Chemo mechanical milling may refer to an impaction process that may form a complex between an organic medium and a nanoparticle. As a result of chemo mechanical milling, the organic medium may coat, encapsulate, or intercalate the nanoparticles.


In another embodiment, the solid lubricant feed may be dry milled and then wet milled. An emulsifier may be mixed with a base and added to the wet milled particles. Dry milling may refer to particles that have been milled in the presence of a vacuum, a gas, or a combination thereof. Wet milling may refer to particles that have been milled in the presence of a liquid.


The solid lubricant nanoparticle composition may further comprise an organic medium. Examples of organic mediums include, but are not limited to, oil mediums, grease mediums, alcohol mediums, or combinations thereof. Specific examples of organic mediums include, but are not limited to, composite oil, canola oil, vegetable oils, soybean oil, corn oil, ethyl and methyl esters of rapeseed oil, distilled monoglycerides, monoglycerides, diglycerides, acetic acid esters of monoglycerides, organic acid esters of monoglycerides, sorbitan, sorbitan esters of fatty acids, propylene glycol esters of fatty acids, polyglycerol esters of fatty acids, n-hexadecane, hydrocarbon oils, phospholipids, or a combination thereof. Many of these organic media may be environmentally acceptable.


The composition may contain emulsifiers, surfactants, or dispersants. Examples of emulsifiers may include, but are not limited to, emulsifiers having a hydrophilic-lipophilic balance (HLB) from about 2 to about 7; alternatively, a HLB from about 3 to about 5; or alternatively, a HLB of about 4. Other examples of emulsifiers may include, but are not limited to, lecithins, soy lecithins, phospholipids lecithins, detergents, distilled monoglycerides, monoglycerides, diglycerides, acetic acid esters of monoglycerides, organic acid esters of monoglycerides, sorbitan esters of fatty acids, propylene glycol esters of fatty acids, polyglycerol esters of fatty acids, compounds containing phosphorous, compounds containing sulfur, compounds containing nitrogen, or a combination thereof.


A method of making a lubricant is described. The composition may be used as an additive dispersed in a base. Examples of bases may include, but are not limited to, oils, greases, plastics, gels, sprays, or a combination thereof. Specific examples of bases may include, but are not limited to, hydrocarbon oils, vegetable oils, corn oil, peanut oil, canola oil, soybean oil, mineral oil, paraffin oils, synthetic oils, petroleum gels, petroleum greases, hydrocarbon gels, hydrocarbon greases, lithium based greases, fluoroether based greases, ethylenebistearamide, waxes, silicones, or a combination thereof.


Described herein is a method of lubricating or coating an object that is part of an end application with a composition comprising at least one of solid lubricant nanoparticles and an organic medium. Further described is a method of lubricating an object by employing the composition comprising solid lubricant nanoparticles and an organic medium as a delivery mechanism.


Disclosed herein are compositions and methods of preparing nanoparticle based lubricants that, among various advantages, display enhanced dispersion stability and resistance to agglomeration. FIG. 1 illustrates a method of preparing nanoparticle based lubricants or compositions. A solid lubricant feed is introduced via line 210 to a ball milling processor 215. Ball milling is carried out in the processor 215 and the solid lubricant feed is milled to comprise particles having an average particle dimension of less than or equal to about 500 nanometers, suitably less than or equal to about 100 nanometers, suitably less than or equal to about 80 nanometers, and more suitably less than or equal to about 50 nanometers. Alternatively, the ball milling may result in milled solid lubricant particles comprising a mixture, the mixture comprising particles having an average particle dimension of less than or equal to about 500 nanometers, plus larger particles. The ball milling may be high energy ball milling, medium energy ball milling, or combinations thereof. Additionally, in various embodiments the ball milling may be carried out in a vacuum, in the presence of a gas, in the presence of a liquid, in the presence of a second solid, or combinations thereof. The nanoparticle composition may be removed from the processor via line 220. The nanoparticle composition may be a nanoparticle based lubricant.


In alternative embodiments, the ball milling may comprise a first ball milling and at least one more subsequent ball millings, or ball milling and/or other processing as appropriate. Suitably, the ball milling may comprise dry milling followed by wet milling FIG. 2 illustrates a further method 100 of preparing nanoparticle based lubricants where dry milling is followed by wet milling Feed 110 introduces a solid lubricant feed into a ball milling processor 115 where dry ball milling, such as in a vacuum or in air, reduces the solid lubricant feed to particles having an average dimension of the size described above. Line 120 carries the dry milled particles to a wet milling processor 125. Via line 160 the dry milled particles are combined with a composite oil or an organic medium prior to entering the wet milling processor 125. Alternatively, the organic medium and dry milled particles may be combined in the wet milling processor 125. In further alternative embodiments (not shown), the dry milling and wet milling may be carried out in a single processor where the organic medium is supplied to the single processor for wet milling after initially carrying out dry milling. In other alternative embodiments, the balls in the ball milling apparatus may be coated with the organic medium to incorporate the organic medium in the solid lubricant nanoparticles.


After wet milling, line 130 carries the wet milled particles to a container 135, which may be a sonication device. Alternatively, line 130 may carry a mixture comprising solid lubricant nanoparticles, organic medium, and a complex comprising the solid lubricant nanoparticles combined with an organic medium.


In another embodiment, prior to introduction of the wet milled particles into the container 135, a base may be fed to the container 135 via line 150. Alternatively, the base may be supplied to the wet milling processor 125 and the mixing, which may include sonicating, may be carried out in the wet milling processor 125. In such embodiments the solid lubricant nanoparticle composition may be employed as an additive and dispersed in the base. A base may be paired with a solid lubricant nanoparticle composition according to the ability of the base and the solid lubricant nanoparticle composition to blend appropriately. In such cases the solid lubricant nanoparticle composition may enhance performance of the base.


In a further embodiment, an emulsifier may be mixed with the base. Emulsifiers may further enhance dispersion of the solid lubricant nanoparticle composition in the base. The emulsifier may be selected to enhance the dispersion stability of a nanoparticle composition in a base. An emulsifier may also be supplied to the container 135 via line 140. In many embodiments, the emulsifier and base are combined in the container 135 prior to introduction of the wet milled particles. Prior mixing of the emulsifier with the base may enhance dispersion upon addition of complexes of solid lubricant nanoparticles and organic medium and/or solid lubricant nanoparticles by homogeneously dispersing/dissolving the complexes/nanoparticles. In some embodiments, the mixing of the emulsifier and base may comprise sonicating. Alternatively, the emulsifier may be supplied to the wet milling processor 125 and the mixing, which may include sonicating, may be carried out in the wet milling processor 125. The lubricant removed from the container 135 via line 120 may be a blend comprising the wet milled particles, organic medium, and base. The blend may further comprise an emulsifier. In other alternative embodiments, additives may be added to the nanoparticle based lubricant during interaction with a mating surface.


In a further embodiment, antioxidants or anticorrosion agents may be milled with the solid lubricant nanoparticles. Examples of antioxidants include, but are not limited to, hindered phenols, alkylated phenols, alkyl amines, aryl amines, 2,6-di-tert-butyl-4-methylphenol, 4,4′-di-tert-octyldiphenylamine, tert-Butyl hydroquinone, tris(2,4-di-tert-butylphenyl)phosphate, phosphites, thioesters, or a combination thereof. Examples of anticorrosion agents include, but are not limited to, alkaline-earth metal bisalkylphenolsulphonates, dithiophosphates, alkenylsuccinic acid half-amides, or a combination thereof. In another embodiment, biocidals may be milled with the solid lubricant nanoparticles. Examples of biocidals may include, but are not limited to, alkyl or kydroxylamine benzotriazole, an amine salt of a partial alkyl ester of an alkyl, alkenyl succinic acid, or a combination thereof.


In yet another embodiment, further processing of wet milled particles may comprise removal of oils that are not a part of a complex with the solid lubricant particles. Such methods may be suitable for applications that benefit from use of dry particles of solid lubricant, such as coating applications. Oil and/or other liquids can be removed from wet milled particles to produce substantially dry solid lubricant particles and complexes. Such wet milling followed by drying may produce a solid lubricant with reduced tendency to agglomerate. In specific embodiments, an agent, such as acetone, can be added that dissolves oils that are not a part of a complex, followed by a drying process such as supercritical drying, to produce a substantially dry solid lubricant comprising particles treated by milling in an organic medium.


Ball milling conditions may vary and, in particular, conditions such as temperature, milling time, and size and materials of the balls and vials may be manipulated. In various embodiments, ball milling may be carried out from about 12 hours to about 50 hours, suitably from about 36 hours to about 50 hours, suitably from about 40 hours to about 50 hours, and more suitably at about 48 hours. Suitably, ball milling is conducted at room temperature. The benefits of increasing milling time may comprise at least one of increasing the time for the organic medium and solid lubricant nanoparticles to interact; and producing finer sizes, better yield of nanoparticles, more uniform shapes, and more passive surfaces. An example of ball milling equipment suitable for carrying out the described milling includes the SPEX CertiPrep model 8000D, along with hardened stainless steel vials and hardened stainless steel grinding balls, but any type of ball milling apparatus may be used. In one embodiment, a stress of 600-650 MPa, a load of 14.9 N, and a strain of 10−3-10−4 per sec may be used.


The proportions of the components in a nanoparticle based lubricant may contribute to performance of the lubricant, such as the lubricants dispersion stability and ability to resist agglomeration. In wet milling, suitable ratios of solid lubricant nanoparticles to organic medium may be about 1 part particles to about 4 parts organic medium by weight, suitably, about 1 part particles to about 3 parts organic medium by weight, suitably, about 3 parts particles to about 8 parts organic medium by weight, suitably, about 2 parts particles to about 4 parts organic medium by weight, suitably, about 1 part particles to about 2 parts organic medium by weight, and suitably, about 1 part particles to about 1.5 parts organic medium by weight.


Suitable ratios of organic medium to emulsifier in a lubricant including the solid lubricant nanoparticles may be about 1 part organic medium to less than or equal to about 1 part emulsifier, suitably, about 1 part organic medium to about 0.5 parts emulsifier by weight, or suitably, from about 0.4 to about 1 part emulsifier for about 1 part organic medium by weight.


The amount of solid lubricant nanoparticle composition (by weight) sonicated or dispersed in the base may be from about 0.25% to about 5%, suitably 0.5% to about 3%, suitably 0.5% to about 2%, and more suitably 0.75% to about 2%.


The amount of emulsifier (by weight) sonicated or dissolved in the base, depending on the end application, shelf-life, and the like, may be from about 0.5% to about 10%, suitably from about 4% to about 8%, suitably from about 5% to about 6%, and suitably, from about 0.75% to about 2.25%.


The solid lubricant nanoparticle composition may be used, without limitation, as lubricants, coatings, delivery mechanisms, or a combination thereof. The solid lubricant nanoparticle composition may be used, without limitation, as an additive dispersed in a base oil. The composition may also be used, without limitation, to lubricate a boundary lubrication regime. A boundary lubrication regime may be a lubrication regime where the average oil film thickness may be less than the composite surface roughness and the surface asperities may come into contact with each other under relative motion. During the relative motion of two surfaces with lubricants in various applications, three different lubrication stages may occur, and the boundary lubrication regime may be the most severe condition in terms of temperature, pressure and speed. Mating parts may be exposed to severe contact conditions of high load, low velocity, extreme pressure (for example, 1-2 GPa), and high local temperature (for example, 150-300 degrees C.). The boundary lubrication regime may also exist under lower pressures and low sliding velocities or high temperatures. In the boundary lubrication regime, the mating surfaces may be in direct physical contact. The composition may further be used, without limitation, as a lubricant or coating in machinery applications, manufacturing applications, mining applications, aerospace applications, automotive applications, pharmaceutical applications, medical applications, dental applications, cosmetic applications, food product applications, nutritional applications, health related applications, bio-fuel applications or a combination thereof. Specific examples of uses in end applications include, without limitation, machine tools, bearings, gears, camshafts, pumps, transmissions, piston rings, engines, power generators, pin-joints, aerospace systems, mining equipment, manufacturing equipment, or a combination thereof. Further specific examples of uses may be, without limitation, as an additive in lubricants, greases, gels, compounded plastic parts, pastes, powders, emulsions, dispersions, or combinations thereof. The composition may also be used as a lubricant that employs the solid lubricant nanoparticle composition as a delivery mechanism in pharmaceutical applications, medical applications, dental applications, cosmetic applications, food product applications, nutritional applications, health related applications, bio-fuel applications, or a combination thereof. The various compositions and methods may also be used, without limitation, in hybrid inorganic-organic materials. Examples of applications using inorganic-organic materials, include, but are not limited to, optics, electronics, ionics, mechanics, energy, environment, biology, medicine, smart membranes, separation devices, functional smart coatings, photovoltaic and fuel cells, photocatalysts, new catalysts, sensors, smart microelectronics, micro-optical and photonic components and systems for nanophotonics, innovative cosmetics, intelligent therapeutic vectors that combined targeting, imaging, therapy, and controlled release of active molecules, and nanoceramic-polymer composites for the automobile or packaging industries.


In some embodiments, the ball milling process may create a close caged dense oval shaped architecture (similar to a football shape or fullerene type architecture). This may occur when molybdenum disulphide is milled in a gas or vacuum. Panel (a) of FIG. 7 shows the close caged dense oval shaped architecture of molybdenum disulphide nanoparticles that have been ball milled in air for 48 hours.


In other embodiments, the ball milling process may create an open ended oval shaped architecture (similar to a coconut shape) of molybdenum disulphide nanoparticles which are intercalated and encapsulated with an organic medium and phospholipids. This may occur when molybdenum disulphide is milled in a gas or vacuum followed by milling in an organic medium. Panel (b) of FIG. 7 shows the open ended oval shaped architecture of molybdenum disulphide nanoparticles that have been ball milled in air for 48 hours followed by ball milling in canola oil for 48 hours.


As shown in the examples, the tribological performance of the nanoparticle based lubricant may be improved. The tribological performance may be measured by evaluating different properties. An anti-wear property may be a lubricating fluid property that has been measured using the industry standard Four-Ball Wear (ASTM D4172) Test. The Four-Ball Wear Test may evaluate the protection provided by an oil under conditions of pressure and sliding motion. Placed in a bath of the test lubricant, three fixed steel balls may be put into contact with a fourth ball of the same grade in rotating contact at preset test conditions. Lubricant wear protection properties may be measured by comparing the average wear scars on the three fixed balls. The smaller the average wear scar, the better the protection. Extreme pressure properties may be lubricating fluid properties that have been measured using the industry standard Four-Ball Wear (ASTM D2783) Test. This test method may cover the determination of the load-carrying properties of lubricating fluids. The following two determinations may be made: 1) load-wear index (formerly Mean-Hertz load) and 2) weld load (kg). The load-wear index may be the load-carrying property of a lubricant. It may be an index of the ability of a lubricant to minimize wear at applied loads. The weld load may be the lowest applied load in kilograms at which the rotating ball welds to the three stationary balls, indicating the extreme pressure level that the lubricants can withstand. The higher the weld point scores and load wear index values, the better the anti-wear and extreme pressure properties of a lubricant. The coefficient of friction (COF) may be a lubricating fluid property that has been measured using the industry standard Four-Ball Wear (ASTM D4172) Test. COF may be a dimensionless scalar value which describes the ratio of the force of friction between two bodies and the force pressing them together. The coefficient of friction may depend on the materials used. For example, ice on metal has a low COF, while rubber on pavement has a high COF. A common way to reduce friction may be by using a lubricant, such as oil or water, which is placed between two surfaces, often dramatically lessening the COF.


The composition may have a wear scar diameter of about 0.4 mm to about 0.5 mm. The composition may have a COF of about 0.06 to about 0.08. The composition may have a weld load of about 150 kg to about 350 kg. The composition may have a load wear index of about 20 to about 40. The values of these tribological properties may change depending on the amount of solid lubricant nanoparticle composition sonicated or dissolved in the base.


Various features and aspects of the invention are set forth in the following examples, which are intended to be illustrative and not limiting.


EXAMPLES
Example 1

Ball milling was performed in a SPEX 8000D machine using hardened stainless steel vials and balls. MoS2 (Alfa Aesar, 98% pure, 700 nm average primary particle size) and canola oil (Crisco) were used as the starting materials in a ratio of 1 part MoS2 (10 grams) to 2 parts canola oil (20 grams). The ball to powder weight ratio was 2 to 1. MoS2 was ball milled for 48 hours in air followed by milling in canola oil for 48 hrs at room temperature. The nanoparticles were about 50 nm after ball milling. Table 1 summarizes milling conditions and resultant particle morphologies. It was observed that there was a strong effect of milling media on the shape of the ball milled nanoparticles. Dry milling showed buckling and folding of the planes when the particle size was reduced from micron size to nanometer size. However, the dry milling condition used here produced micro clusters embedding several nanoparticles. On the other hand, wet milling showed no buckling but saw de-agglomeration.









TABLE 1







Milling conditions and parametric effect on particle size and shape










Shape of the particles
Shape of the clusters













Dry




Milling


12 hours
Plate-like with sharp edges
Sharp and irregular


24 hours
Plate-like with round edges
More or less rounded


48 hours
Spherical
Globular clusters


Wet


Milling


12 hours
Thin plates with sharp edges
Thing plates with sharp edges


24 hours
Thin plates with sharp edges
Thin plates with sharp edges


48 hours
Thin plates with sharp edges
Thin plates with sharp edges
















TABLE 2







Effect of milling media on resultant size (starting size


sub-micron), shape, and agglomeration of particles















Dry milled and


Properties
Dry
Alcohol
Oil
oil milled














Clusters size (nm)
100
300
200
100


Particle size (nm)
30
80
80
30


Agglomeration
High
Very less
Very less
Very less


Shape of the
Spherical
Platelet
Platelet
Spherical


particles










FIG. 3 shows TEM micrographs of the as-available (700 nm), air milled, and hybrid milled (48 hrs in air medium followed by 48 hours in oil medium) MoS2 nanoparticles. Panel (A) represents micron-sized particle chunks of the as-available MoS2 sample off the shelf. These micrographs, particularly panel (B), represent agglomerates of lubricant nanoparticles when milled in the air medium. Panel (B) clearly demonstrates size reduction in air milled MoS2. Higher magnification (circular regions) revealed formation of the disc shaped nanoparticles after milling in the air medium. From panels (C) and (D) it may be concluded that the particle size was reduced to less than 30 nm after milling in air and hybrid conditions. Regardless of the occasionally observed clusters, the average size of the clusters is less than or equal to 200 nm.


Hybrid milled samples were dispersed in paraffin oil (from Walmart) and remained suspended without settling. However, the dispersion was not uniform after a few weeks. To stabilize the dispersion and extend the anti-wear properties, phospholipids were added. Around 2% by weight of soy lecithin phospholipids (from American Lecithin) was added in the base oil.



FIGS. 4 and 5 show the XRD and XPS spectra of MoS2 before and after ball milling, respectively. XRD spectra revealed no phase change as well as no observable amorphization in the MoS2 after milling. This observation is consistent with the continuous platelets observed throughout the nanoparticle matrix in TEM analysis for milled material. Broadening of peaks (FWHM) was observed in XRD spectra of MoS2 ball milled in air and hybrid media, respectively. The peak broadening may be attributed to the reduction in particle size. The estimated grain size is 6 nm. This follows the theme of ball milling where clusters consist of grains and sub-grains of the order of 10 nm. XPS analysis was carried out to study the surface chemistry of the as-available and hybrid milled MoS2 nanoparticles. As shown in FIG. 5, a carbon (C) peak observed at 285 eV in the as-available MoS2 sample shifted to 286.7 eV. Bonding energies of 286 eV and 287.8 eV correspond to C—O and C═O bond formation, respectively. The observed binding energy level may demonstrate that a thin layer containing mixed C—O & C═O groups enfolds the MoS2 particles.


Preliminary tribological tests on the synthesized nanoparticles were performed on a four-ball machine by following ASTM 4172. The balls used were made of AISI 52100 stainless steel and were highly polished. Four Ball Wear Scar measurements using ASTM D4172 were made under the following test conditions:



















Test Temperature, ° C.
75
(±1.7)



Test Duration, min
60
(±1)



Spindle Speed, rpm
1,200
(±60)



Load, kg
40
(±0.2)











Wear scar diameter (WSD, mm) of each stationary ball was quantified in both vertical and horizontal directions. The average value of WSD from 3 independent tests was reported within ±0.03 mm accuracy.


Four Ball Extreme Pressure measurements using ASTM D2783 were made under the following test conditions:


















Test Temperature, ° C.
23



Test Duration, min

60 (±1)




Spindle Speed, rpm
1,770 (±60)



Load, kg
Varies, 10-sec/stage



Ball Material
AISI-E52100



Hardness
64-66



Grade
25EP










Three different particles (in w/w ratio) were evaluated for their anti-wear properties as additives in paraffin oil. FIG. 6(A) shows the average wear scar measurements for paraffin oil without a nanoparticle additive, paraffin oil with micron sized MoS2, paraffin oil with MoS2 that was milled in air for 48 hours, and paraffin oil with MoS2 that was milled in air for 48 hours followed by milling in canola oil for 48 hours. FIG. 6(B) shows the load wear index for paraffin oil without a nanoparticle additive, paraffin oil with micron sized MoS2, paraffin oil with MoS2 that was milled in air for 48 hours, and paraffin oil with MoS2 that was milled in air for 48 hours followed by milling in canola oil for 48 hours. FIG. 6(C) shows the COF for paraffin oil without a nanoparticle additive, paraffin oil with micron sized MoS2, paraffin oil with MoS2 that was milled in air for 48 hours, and paraffin oil with MoS2 that was milled in air for 48 hours followed by milling in canola oil for 48 hours. FIG. 6(D) shows the extreme pressure data for paraffin oil with micron sized MoS2, paraffin oil with MoS2 that was milled in air for 48 hours, and paraffin oil with MoS2 that was milled in air for 48 hours followed by milling in canola oil for 48 hours. In each test the nanoparticle additive was present in the amount of 1% by weight.


Test Data from Nanoparticle Composition Additive in Base Oil











Test data from nanoparticle composition additive in base oil












Four Ball Extreme pressure



Solid Lubricant
Four Ball Tests at 40 kg Load
(ASTM D-2783)











All dispersions diluted to x %
(ASTM D4172)
Weld Load
Load Wear
FIG. 6(A)












by wt. in reference base oil
WSD (mm)
COF
(kg)
Index
amd 6(B)





Paraffin oil
1.033
0.155
126
12.1
A


Nanoparticles of MoS2
1.012
0.102
100
16.1
B


without organic medium


(0.5%)


Nanoparticles of MoS2
0.960
0.114
126
20.8
C


without organic medium


(1.0%)


Nanoparticles of MoS2
0.915
0.098
126
22.0
D


without organic medium


(1.5%)


Conventional available micro
1.009
0.126
160
22.0
E


particles (0.5%)


Conventional available micro
0.948
0.091
126
19.1
F


particles (1.0%)


Conventional available micro
0.922
0.106
126
16.5
G


particles (1.5%)


NanoGlide: Nanoparticles of
0.451
0.077
160
24.8
H


MoS2 with organic medium


(0.5%)


NanoGlide: Nanoparticles of
0.461
0.069
200
25.9
I


MoS2 with organic medium


(1.0%)


NanoGlide: Nanoparticles of
0.466
0.075
315
34.3
J


MoS2 with organic medium


(1.5%)









The transfer film in the wear scar, studied using energy dispersive x-ray analysis (EDS), identified the signatures of phosphates in addition to molybdenum and sulfur. Panel (a) of FIG. 9 depicts the base case of paraffin oil without a nanoparticle additive. Panel (b) of FIG. 9 depicts paraffin oil with the molybdenum disulfide nanoparticles and the emulsifier. It shows the early evidences of molybdenum (Mo)-sulfur (S)-phosphorous (P) in the wear track. Iron (Fe) is seen in panels (a) and (b) of FIG. 9, as it is the material of the balls (52100 steel) in the four-ball test. The molybdenum and sulfur peaks coincide and are not distinguishable because they have the same binding energy. Elemental mapping also showed similar results.


Prophetic Examples

Examples 2-23 are made using a similar method as Example 1, unless specified otherwise.


Example 2

MoS2 (Alfa Aesar, 98% pure, 700 nm average particle size) and canola oil from ADM are used as the starting materials. The MoS2 powder is ball milled for various time conditions, variable ball/powder ratios, and under various ambient conditions, starting with air, canola oil and the subsequent combination of milling in air followed by milling in canola oil. It is also ball milled in different types of organic media. For example, one organic medium that is used is canola oil methyl ester. The processing of this will be similar to the above mentioned example.


Different types of ball milling processes can be used. For instance, in the first step, cryo ball milling in air followed by high temperature ball milling in an organic medium is used.


After the ball milling, the active EP-EA (extreme pressure—environmentally acceptable) particles are treated with phospholipids that have been mixed with a base oil such as paraffin oil.


Example 3

Molybdenum disulphide is ball milled with boron using a ratio of 1 part molybdenum disulphide to 1 part boron. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-boron-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 4

Molybdenum disulphide is ball milled with copper using a ratio of 1 part molybdenum disulphide to 1 part metal. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-copper-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 5

A molybdenum disulphide/graphite (obtained from Alfa Aesar) mixture in the ratio of 1:1 is ball milled. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-graphite-canola oil) to 2 parts emulsifier. This is added to the base oil paraffin oil).


Example 6

A molybdenum disulphide/boron nitride (Alfa Aesar) mixture in the ratio of 1:1 mixture is ball milled. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-boron nitride-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 7

A molybdenum disulphide/graphite/boron nitride mixture in the ratio 1:1:1 is ball milled. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-graphite-boron nitride-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 8

A molybdenum disulphide/graphite mixture in the ratio of 1:1:1 is ball milled. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-graphite-boron-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 9

A molybdenum disulphide/graphite mixture in the ratio of 1:1 is ball milled with copper using a ratio of 1 part molybdenum disulphide/graphite to 1 part metal. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-graphite-copper-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 10

A molybdenum disulphide/boron nitride mixture in the ratio of 1:1 is ball milled with boron using a ratio of 1 part molybdenum disulphide/boron nitride to 1 part metal. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-boron nitride-boron-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 11

A molybdenum disulphide/boron nitride mixture in the ratio of 1:1 mixture is ball milled with copper using a ratio of 1 part molybdenum disulphide/boron nitride to 1 part metal. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-boron nitride-copper-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 12

A molybdenum disulphide/boron nitride/graphite mixture in the ratio of 1:1:1 is ball milled with boron using a ratio of 1 part molybdenum disulphide/boron nitride/graphite to 1 part metal. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-boron nitride-graphite-boron-Canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 13

A molybdenum disulphide/boron nitride/graphite in the ratio of 1:1:1 is ball milled with copper using a ratio of 1 part molybdenum disulphide/boron nitride/graphite to 1 part metal. This mixture is then ball milled with vegetable oil (canola oil) using a ratio of 1 part solid lubricant nanoparticles to 1.5 parts canola oil. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-boron nitride-graphite-copper-canola oil) to 2 parts emulsifier. This is added to the base oil (paraffin oil).


Example 14

Molybdenum disulphide is ball milled with polytetrafluoroethylene (Teflon®) in a ration of 1 part molybdenum disulphide to 1 part Teflon®. This mixture is then added to the base oil (paraffin oil) with a phospholipid emulsifier (soy lecithin).


Example 15

Molybdenum disulphide is ball milled with polytetrafluoroethylene (Teflon®) in a ration of 1 part molybdenum disulphide to 1 part Teflon®. This mixture is then added to the base oil (paraffin oil) with a phospholipid emulsifier (soy lecithin).


Example 16

Molybdenum disulphide is ball milled with metal additives like copper, silver, lead etc. in a ratio of 1 part molybdenum disulphide to 1 part metal additive. This mixture is further ball milled in vegetable oil based esters (canola oil methyl esters) in a ratio of 1 part solid lubricant nanoparticles to 1.5 parts esters. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-esters) to 2 parts phospholipid emulsifier. This is added to the base oil (paraffin oil).


Example 17

Molybdenum disulphide is ball milled with metal additives like copper, silver, lead etc. in a ratio of 1 part molybdenum disulphide to 1 part metal additive. This mixture is further ball milled in vegetable oil based esters (canola oil methyl esters) in a ratio of 1 part solid lubricant nanoparticles to 1.5 parts esters. This is added to the base oil (paraffin oil).


Example 18

Molybdenum disulphide is ball milled. The solid lubricant nanoparticles are further ball milled in vegetable oil based esters (canola oil methyl esters) in a ratio of 1 part solid lubricant nanoparticles to 1.5 parts esters. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-esters) to 2 parts phospholipid emulsifier. This is added to the base oil (paraffin oil).


Example 19

Molybdenum disulphide is ball milled. The solid lubricant nanoparticles are further ball milled in vegetable oil based esters (canola oil methyl esters) in a ratio of 1 part solid lubricant nanoparticles to 1.5 parts esters. This is added to the base oil (paraffin oil).


Example 20

Molybdenum disulphide is ball milled with metal additives like copper, silver, lead etc. in a ratio of 1 part molybdenum disulphide to 1 part metal additive. This mixture is further ball milled in fatty acids (oleic acid) in a ratio of 1 part solid lubricant nanoparticles to 1.5 parts fatty acids. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-oleic acid) to 2 parts phospholipid emulsifier. This is added to the base oil (paraffin oil).


Example 21

Molybdenum disulphide is ball milled with metal additives like copper, silver, lead etc. in a ratio of 1 part molybdenum disulphide to 1 part metal additive. This mixture is further ball milled in fatty acids (oleic acid) in a ratio of 1 part solid lubricant nanoparticles to 1.5 parts fatty acids. This is added to the base oil (paraffin oil).


Example 22

Molybdenum disulphide is ball milled. The solid lubricant nanoparticles are further ball milled in fatty acids (oleic acid) in a ratio of 1 part solid lubricant nanoparticles to 1.5 parts fatty acids. An emulsifier is added using a ratio of 1 part solid lubricant nanoparticle composition (MoS2-oleic acid) to 2 parts phospholipid emulsifier. This is added to the base oil (paraffin oil).


Example 23

Molybdenum disulphide is ball milled. The solid lubricant nanoparticles are further ball milled in fatty acids (oleic acid) in a ratio of 1 part solid lubricant nanoparticles to 1.5 parts fatty acids. This is added to the base oil (paraffin oil).

Claims
  • 1. An additive package comprising a multifunctional additive macromolecule comprising: a plurality of lubricant nanoparticles having an open-ended architecture; andan organic medium intercalated in the nanoparticles; andwherein at least a portion of the nanoparticles have an average particle dimension of less than or equal to about 500 nm.
  • 2. The additive package of claim 1, wherein the nanoparticles comprise one or more of a layered material, molybdenum disulphide, tungsten disulphide, graphite, polytetrafluoroethylene, boron nitride, hexagonal boron nitride, a soft metal, silver, lead, nickel, copper, cerium fluoride, zinc oxide, silver sulfate, cadmium iodide, lead iodide, barium fluoride, tin sulfide, zinc phosphate, zinc sulfide, mica, boron nitrate, borax, fluorinated carbon, zinc phosphide, and boron.
  • 3. The additive package of claim 1, wherein the organic medium comprises one or more of an oil medium, a grease medium, an alcohol medium, a composite oil, a canola oil, a vegetable oil, a soybean oil, a corn oil, an ethyl and methyl ester of rapeseed oil, a distilled monoglyceride, a monoglyceride, a diglyceride, an acetic acid ester of monoglyceride, an organic acid ester of monoglyceride, a sorbitan, a sorbitan ester of fatty acid, a propylene glycol ester of fatty acid, a polyglycerol ester of fatty acid, a hydrocarbon oil, a n-hexadecane, and a phospholipid.
  • 4. The additive package of claim 1, wherein the additive package is added to at least one material.
  • 5. The additive package of claim 4, wherein the at least one material is a base comprising one or more of an oil, a grease, a plastic, a gel, a spray, a hydrocarbon oil, a vegetable oil, a corn oil, a peanut oil, a canola oil, a soybean oil, a mineral oil, a paraffin oil, a synthetic oil, a petroleum gel, a petroleum grease, a hydrocarbon gel, a hydrocarbon grease, a lithium based grease, a fluoroether based grease, an ethylenebistearamide, a wax, and a silicone.
  • 6. The additive package of claim 4, wherein the at least one material comprises a greaseless material.
  • 7. The additive package of claim 4, wherein the at least one material comprises an emulsifier, wherein the emulsifier comprises one or more of a lecithin, a phospholipid, a soy lecithin, a detergent, a distilled monoglyceride, a monoglyceride, a diglyceride, an acetic acid ester of monoglyceride, an organic acid ester of monoglyceride, a sorbitan ester of fatty acid, a propylene glycol ester of fatty acid, a polyglycerol ester of fatty acid, a compound containing phosphorous, a compound containing sulfur, and a compound containing nitrogen.
  • 8. The additive package of claim 4, wherein the at least one material comprises an antioxidant.
  • 9. The additive package of claim 8, wherein the antioxidant comprises one or more of a hindered phenol, an alkylated phenol, an alkyl amine, an aryl amine, a 2,6-di-tert-butyl-4-methylphenol, a 4,4′-di-tert-octyldiphenylamine, a tert-butyl hydroquinone, a tris(2,4-di-tert-butylphenyl)phosphate, a phosphite, and a thioester.
  • 10. The additive package of claim 4, wherein the at least one material comprises a corrosion inhibitor material.
  • 11. The additive package of claim 10, wherein the corrosion inhibitor material comprises one or more of an alkaline-earth metal bisalkylphenolsulphonate, a dithiophosphate, and an alkenylsuccinic acid half-amide.
  • 12. The additive package of claim 1, wherein the organic medium comprises a greaseless material.
  • 13. The additive package of claim 1, wherein the additive package is greaseless.
  • 14. The additive package of claim 1, wherein the additive package is added to the at least one material in order to form a lubricant or a coating; and wherein the lubricant or the coating is in contact with at least a portion of a surface of an object.
  • 15. A method comprising: adding an additive package to at least one material, the additive package comprising a multifunctional additive macromolecule comprising: a plurality of lubricant nanoparticles having an open-ended architecture; andan organic medium intercalated in the nanoparticles; andwherein at least a portion of the nanoparticles have an average particle dimension of less than or equal to about 500 nm.
  • 16. The method of claim 15, wherein the nanoparticles comprise one or more of a layered material, molybdenum disulphide, tungsten disulphide, graphite, polytetrafluoroethylene, boron nitride, hexagonal boron nitride, a soft metal, silver, lead, nickel, copper, cerium fluoride, zinc oxide, silver sulfate, cadmium iodide, lead iodide, barium fluoride, tin sulfide, zinc phosphate, zinc sulfide, mica, boron nitrate, borax, fluorinated carbon, zinc phosphide, and boron.
  • 17. The method of claim 15, wherein the organic medium comprises one or more of an oil medium, a grease medium, an alcohol medium, a composite oil, a canola oil, a vegetable oil, a soybean oil, a corn oil, an ethyl and methyl ester of rapeseed oil, a distilled monoglyceride, a monoglyceride, a diglyceride, an acetic acid ester of monoglyceride, an organic acid ester of monoglyceride, a sorbitan, a sorbitan ester of fatty acid, a propylene glycol ester of fatty acid, a polyglycerol ester of fatty acid, a hydrocarbon oil, a n-hexadecane, and a phospholipid.
  • 18. The method of claim 15, wherein the at least one material is a base comprising one or more of an oil, a grease, a plastic, a gel, a spray, a hydrocarbon oil, a vegetable oil, a corn oil, a peanut oil, a canola oil, a soybean oil, a mineral oil, a paraffin oil, a synthetic oil, a petroleum gel, a petroleum grease, a hydrocarbon gel, a hydrocarbon grease, a lithium based grease, a fluoroether based grease, an ethylenebistearamide, a wax, and a silicone.
  • 19. The method of claim 15, wherein the at least one material comprises a greaseless material.
  • 20. The method of claim 15, wherein the at least one material comprises an emulsifier or a dispersant.
  • 21. The method of claim 20, wherein the at least on material comprises the emulsifier, and wherein the emulsifier comprises one or more of a lecithin, a phospholipid, a soy lecithin, a detergent, a distilled monoglyceride, a monoglyceride, a diglyceride, an acetic acid ester of monoglyceride, an organic acid ester of monoglyceride, a sorbitan ester of fatty acid, a propylene glycol ester of fatty acid, a polyglycerol ester of fatty acid, a compound containing phosphorous, a compound containing sulfur, and a compound containing nitrogen.
  • 22. The method of claim 15, wherein the at least one material comprises an antioxidant.
  • 23. The method of claim 22, wherein the antioxidant comprises one or more of a hindered phenol, an alkylated phenol, an alkyl amine, an aryl amine, a 2,6-di-tert-butyl-4-methylphenol, a 4,4′-di-tert-octyldiphenylamine, a tert-butyl hydroquinone, a tris(2,4-di-tert-butylphenyl)phosphate, a phosphite, and a thioester.
  • 24. The method of claim 15, wherein the at least one material comprises a corrosion inhibitor material.
  • 25. The method of claim 24, wherein the corrosion inhibitor material comprises one or more of an alkaline-earth metal bisalkylphenolsulphonate, a dithiophosphate, and an alkenylsuccinic acid half-amide.
  • 26. The method of claim 15, wherein the organic medium comprises a greaseless material.
  • 27. The method of claim 15, wherein the additive package is greaseless.
  • 28. The method of claim 15, wherein adding the additive package to the at least one material forms a coating, and wherein the method further comprises adding the coating to at least a portion of a surface of an object.
  • 29. The method of claim 15, wherein adding the additive package to the at least one material forms a lubricant, and wherein the method further comprises adding the lubricant to at least a portion of a surface of an object.
  • 30. An additive package comprising: a lubricant nanoparticle having an open-ended architecture; andan organic medium intercalated in the nanoparticle; andwherein the nanoparticle has a particle dimension of less than or equal to about 500 nm.
CROSS-REFERENCE TO RELATED APPLICATIONS

This patent application is a continuation application and claims the benefit of the filing date under 35 U.S.C. §120 of U.S. patent application Ser. No. 13/921,640, filed on Jun. 19, 2013. U.S. patent application Ser. No. 13/921,640 is a continuation application and claims the benefit of the filing date under 35 U.S.C. §120 of U.S. patent application Ser. No. 12/160,758, filed on Sep. 2, 2008. U.S. patent application Ser. No. 12/160,758 is a national stage filing under 35 U.S.C. §371 and claims priority to International Application No. PCT/US2007/060506, filed on Jan. 12, 2007. International Application No. PCT/US2007/060506 claims priority under 35 U.S.C. §119(e) to U.S. Provisional Patent Application No. 60/758,307, filed on Jan. 12, 2006, which is hereby fully incorporated by reference.

STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT

This invention was made with U.S. government support under grant number NSF/DMI 0115532 awarded in part by the National Science Foundation. The U.S. government has certain rights in the invention.

US Referenced Citations (197)
Number Name Date Kind
3172892 La Suer Mar 1965 A
3666662 Lowe May 1972 A
3883314 Schnyder et al. May 1975 A
4105571 Shaub et al. Aug 1978 A
4168241 Kozima et al. Sep 1979 A
4223958 Gray Sep 1980 A
4334928 Hara et al. Jun 1982 A
4715972 Pacholke Dec 1987 A
4745010 Sarin et al. May 1988 A
4816334 Yokoyama et al. Mar 1989 A
4877677 Hirochi et al. Oct 1989 A
5129918 Chattopadhay Jul 1992 A
5273790 Herb et al. Dec 1993 A
5286565 Holzl et al. Feb 1994 A
5328875 Ueda et al. Jul 1994 A
5330854 Singh et al. Jul 1994 A
5352501 Miyamoto et al. Oct 1994 A
5363821 Rao et al. Nov 1994 A
5389118 Hinterman et al. Feb 1995 A
5391422 Omori et al. Feb 1995 A
5407464 Kaliski Apr 1995 A
5441762 Gray et al. Aug 1995 A
5466642 Tajima et al. Nov 1995 A
5478622 Nakamura et al. Dec 1995 A
5500331 Czekai et al. Mar 1996 A
5503913 Konig et al. Apr 1996 A
5523006 Strumban Jun 1996 A
5534808 Takaki et al. Jul 1996 A
5536577 Murayama et al. Jul 1996 A
5614140 Pinneo Mar 1997 A
5671532 Rao et al. Sep 1997 A
5677060 Terentieva et al. Oct 1997 A
5704556 McLaughlin Jan 1998 A
5766783 Utsumi et al. Jun 1998 A
5800866 Myers et al. Sep 1998 A
5830577 Murayama et al. Nov 1998 A
5830813 Yao et al. Nov 1998 A
5834689 Cook Nov 1998 A
5882777 Kukino et al. Mar 1999 A
5889219 Moriguchi Mar 1999 A
5897751 Makowiecki et al. Apr 1999 A
5902671 Kutscher May 1999 A
5928771 DeWald, Jr. et al. Jul 1999 A
5945166 Singh et al. Aug 1999 A
6123923 Unger et al. Sep 2000 A
6146645 Deckers et al. Nov 2000 A
6183762 Deckers et al. Feb 2001 B1
6196910 Johnson et al. Mar 2001 B1
6210742 Deckers et al. Apr 2001 B1
6217843 Homyonfer et al. Apr 2001 B1
6258139 Jensen Jul 2001 B1
6258237 Gal-Or et al. Jul 2001 B1
6267989 Liversidge Jul 2001 B1
6370762 Li et al. Apr 2002 B1
6372012 Majagi et al. Apr 2002 B1
6383404 Sakai et al. May 2002 B1
6395634 Miyamoto May 2002 B1
6410086 Brandon et al. Jun 2002 B1
6484826 Anderson et al. Nov 2002 B1
6540800 Sherman et al. Apr 2003 B2
6544599 Brown et al. Apr 2003 B1
6548139 Sakai et al. Apr 2003 B2
6548264 Tan et al. Apr 2003 B1
6607782 Malshe et al. Aug 2003 B1
6652967 Yadav et al. Nov 2003 B2
6709622 Billiet et al. Mar 2004 B2
6710020 Tenne et al. Mar 2004 B2
6878676 Migdal et al. Apr 2005 B1
6895855 Doll May 2005 B2
6933049 Wan et al. Aug 2005 B2
6933263 Manka et al. Aug 2005 B2
6945699 Tibbits Sep 2005 B2
6951583 Clere et al. Oct 2005 B2
6962895 Scharf et al. Nov 2005 B2
6962946 Brady et al. Nov 2005 B2
6976647 Reed et al. Dec 2005 B2
7018606 Tenne et al. Mar 2006 B2
7018958 Arrowsmith et al. Mar 2006 B2
7022653 Hartley et al. Apr 2006 B2
7244498 Cook et al. Jul 2007 B2
7335245 He et al. Feb 2008 B2
7371474 Liu et al. May 2008 B1
7372615 Chen et al. May 2008 B2
7374473 Kumasaka et al. May 2008 B2
7375060 Kuzmin et al. May 2008 B2
7387813 Kumar et al. Jun 2008 B2
7410697 Schneider et al. Aug 2008 B2
7419941 Waynick Sep 2008 B2
7430359 Chen et al. Sep 2008 B2
7438976 He et al. Oct 2008 B2
7449432 Lockwood et al. Nov 2008 B2
7458384 Seal et al. Dec 2008 B1
7463404 Chen et al. Dec 2008 B2
7470650 Zhang et al. Dec 2008 B2
7471439 Chen et al. Dec 2008 B2
7494907 Brown et al. Feb 2009 B2
7510760 Malshe et al. Mar 2009 B2
7524481 Tenne et al. Apr 2009 B2
7549938 Leighton et al. Jun 2009 B2
7556743 Furman et al. Jul 2009 B2
7571774 Shuster et al. Aug 2009 B2
7580174 Chen et al. Aug 2009 B2
7594962 Bujard et al. Sep 2009 B2
7597950 Stellacci et al. Oct 2009 B1
7614270 Luckey, Jr. et al. Nov 2009 B2
7616370 Chen et al. Nov 2009 B2
7641886 Tenne et al. Jan 2010 B2
7687112 Buehler et al. Mar 2010 B2
7704125 Roy et al. Apr 2010 B2
7723812 Chen et al. May 2010 B2
7749562 Lam et al. Jul 2010 B1
7763489 Chen et al. Jul 2010 B2
7767632 Esche, Jr. et al. Aug 2010 B2
7768366 Patton et al. Aug 2010 B1
7771821 Martin et al. Aug 2010 B2
7790658 Sawyer et al. Sep 2010 B2
7803347 Ajiri Sep 2010 B2
7816297 Lee Oct 2010 B2
7846556 Erdemir et al. Dec 2010 B2
7871533 Haiping et al. Jan 2011 B1
7952786 Chen et al. May 2011 B2
7955857 Bastide et al. Jun 2011 B2
7959891 Tenne et al. Jun 2011 B2
7968505 Liu et al. Jun 2011 B2
7994105 Narayan Aug 2011 B2
7998572 McGilvray et al. Aug 2011 B2
8048526 Mizrahi Nov 2011 B2
8071160 Chinn et al. Dec 2011 B2
8074906 Talton Dec 2011 B2
8075792 Branz et al. Dec 2011 B1
8076809 Tingler et al. Dec 2011 B2
8114373 Jang et al. Feb 2012 B2
8117902 Santore et al. Feb 2012 B2
8221828 Chinn et al. Jul 2012 B2
8322754 Carcagno et al. Dec 2012 B2
8476206 Malshe Jul 2013 B1
8486870 Malshe Jul 2013 B1
8492319 Malshe et al. Jul 2013 B2
20040076572 Clere et al. Apr 2004 A1
20050002970 Ketelson et al. Jan 2005 A1
20050065044 Migdal et al. Mar 2005 A1
20050124504 Zhang et al. Jun 2005 A1
20050191357 Kawashima et al. Sep 2005 A1
20050287348 Faler Dec 2005 A1
20050288192 Alexander Dec 2005 A1
20060025515 Scaringe et al. Feb 2006 A1
20060040832 Zhang et al. Feb 2006 A1
20060056752 Tibbits Mar 2006 A1
20060120947 Tenne et al. Jun 2006 A1
20060258875 Reyes et al. Nov 2006 A1
20070004602 Waynick Jan 2007 A1
20070158609 Hong et al. Jul 2007 A1
20070158610 Hong et al. Jul 2007 A1
20070262120 Coleman et al. Nov 2007 A1
20070293405 Zhang et al. Dec 2007 A1
20080029625 Talton Feb 2008 A1
20080050450 Arnold et al. Feb 2008 A1
20080066375 Roos et al. Mar 2008 A1
20080161213 Jao et al. Jul 2008 A1
20080234149 Malshe et al. Sep 2008 A1
20080269086 Adhvaryu Oct 2008 A1
20080287326 Zhang et al. Nov 2008 A1
20090014691 Kint et al. Jan 2009 A1
20090018037 Mabuchi et al. Jan 2009 A1
20090048129 Mabuchi et al. Feb 2009 A1
20090053268 DePablo et al. Feb 2009 A1
20090074522 Graham et al. Mar 2009 A1
20090118148 Martin et al. May 2009 A1
20090155479 Xiao et al. Jun 2009 A1
20090169745 Nohr et al. Jul 2009 A1
20090170733 Hwang et al. Jul 2009 A1
20090246285 Stellacci et al. Oct 2009 A1
20100029518 Markovitz et al. Feb 2010 A1
20100092663 Ajiri Apr 2010 A1
20100099590 Liu Apr 2010 A1
20100112073 Sabliov et al. May 2010 A1
20100204072 Kwon et al. Aug 2010 A1
20100227782 Tenne et al. Sep 2010 A1
20100261625 Hakamata Oct 2010 A1
20100298180 Patel et al. Nov 2010 A1
20110052934 Sugimoto et al. Mar 2011 A1
20110118156 Rühle et al. May 2011 A1
20110136708 Mabuchi et al. Jun 2011 A1
20110166051 Mizrahi et al. Jul 2011 A1
20110172132 Branson et al. Jul 2011 A1
20110206596 Tenne et al. Aug 2011 A1
20110229580 Srivastava et al. Sep 2011 A1
20110244692 Jeong et al. Oct 2011 A1
20110257054 Baran, Jr. et al. Oct 2011 A1
20110287987 Mordukhovich et al. Nov 2011 A1
20120032543 Chakraborty et al. Feb 2012 A1
20140024565 Malshe et al. Jan 2014 A1
20140038862 Hague et al. Feb 2014 A1
20140212587 Malshe Jul 2014 A1
20140364348 Malshe Dec 2014 A1
20150132539 Bailey May 2015 A1
20150361375 Malshe Dec 2015 A1
Foreign Referenced Citations (15)
Number Date Country
1080648 Jan 1994 CN
63-040708 Feb 1988 JP
10130678 May 1998 JP
10195473 Jul 1998 JP
10330779 Dec 1998 JP
2002-294272 Oct 2002 JP
2006045350 Feb 2006 JP
WO 9502025 Jan 1995 WO
WO 9824833 Aug 1998 WO
WO 2005060648 Jul 2005 WO
WO 2005060648 Jul 2005 WO
WO 2006076725 Jul 2006 WO
WO 2006134061 Dec 2006 WO
WO 2007082299 Jul 2007 WO
WO 2014008006 Jan 2014 WO
Non-Patent Literature Citations (38)
Entry
USPTO Office Action for U.S. Appl. No. 11/074,597, filed Mar. 20, 2008.
USPTO Office Action for U.S. Appl. No. 11/074,597, filed Aug. 23, 2007.
USPTO Office Action for U.S. Appl. No. 11/074,597, filed Jan. 31, 2007.
USPTO Office Action for U.S. Appl. No. 12/007,555, filed Jan. 12, 2010.
USPTO Office Action for U.S. Appl. No. 12/007,555, filed Oct. 4, 2012.
Supplemental European Extended Search Report and Search Opinion for European Patent Application No. 07710113.7 dated Sep. 20, 2012.
English translation of Japanese Office Action for Application No. 2008-550538 dated Sep. 20, 2012.
International Search Report, issued Oct. 16, 2015 in PCT/US15/27925.
Bakunin, V.N. et al., “Synthesis and application of inorganic nanoparticles as lubricant components—a review”, J. Nanoparticle Res (2004) 6:273-284.
Dmytryshyn, S.L. et al., “Synthesis and characterization of vegetable oil derived esters: evaluation for their diesel additive properties”, Bioresource Tech. (2004) 92:55-64.
Hsu, S.M. et al., “Boundary lubricating films: formation and lubrication mechanism”, Tribology Int'l (205) 38:305-312.
Hu, J.J. et al , “Synthesis and microstructural characterization of inorganic fullerene-like MoS2 and graphite-MoS2 hybrid nanoparticles”, J. Mater. Res. (2006) 21(4): 1033-1040.
Jiang, W, et al., “Cubic boron nitride (cBN) based nanocomposite coatings on cutting inserts with chip breakers for hard turning applications”, Surface & Coatings Technology (2005) 200:1849-1854.
Li, B. et al., “Tribochemistry and antiwear mechanism of organic-inorganic nanoparticles as lubricant additives”, Technology Letters (2006) 22(1): 79-84.
Malshe, A.P. et al., “Nanostructured coatings for machining and wear-resistant applications”, JOM (2002) 25-30.
Menezes, P.L. et al., “Studies on friction and transfer later: role of surface texture”, Tribology Letter (2006) 24(3):265-273.
Minami, I. et al., “Antiwear properties of phosphorous-containing compounds in vegetable oils”, Tribology Letter (2002) 13(2):95-101.
Moshkovith, A. et al., “Friction of fullerene-like WS2 nanoparticles; effect of agglomeration”, Tribology Letter (2006) 24(3):225-228.
Ozkan et al., “Femtosecond laser-induced periodic structure writing on diamond crystals and microclusters”, Applied Physics Letters, vol. 75, No. 23, Dec. 6, 1999, pp. 3716-3718.
Rao, C.N.R. et al., “Inorganic nanotubes”, Dalton Trans. (2003) 1-24.
Russell, W.C. et al., “CBN-TiN composite coating using a novel combinational method—structure and performance in metal cutting”, J. Mfg. Sci. Eng. (2003) 125:431-434.
Spikes, H., The thickness, friction and wear of lubricant files, a PowerPoint presentation given at the SAE Powertrain & Fluid Systems Conference and Exhibition, San Antonio. Texas (Oct. 25, 2005).
Verma, A. et al., “Exploring mechanical synthesis of inorganic nanoparticles of MoS2 lubricant and is composite with organic medium for advanced manufacturing”, ISNM (2006) Paper No. 33.
Wu. J.-H. et al., “Bio-inspired surface engineering and tribology of MoS2 overcoateg oBN-TiN composite coating”, Wear (2006) 261(5-6):592-599.
Yedave, S.N. et al., “Novel composite CBN-TiN coating; synthesis and performance analysis”, J. Mfg. Processes (2005) 50:154-162.
Spalvins, T. “A review of recent advances in solid film lubrication”, J. Vac. Sci. Technol/ A (1987) 5(2):212-219.
Canter, Dr. Neil, “EP nanoparticles-based lubricant package”, Tribology & Lubrication Technology. Apr. 2009, pp. 12-17.
Demydov. Ph.D., Dmytro, “Progress Report (2nd Quarter) Advanced Lubrication for Energy Efficiency, Durability and Lower Maintenance Costs of Advanced Naval Components and Systems”, NanoMech, LLC, prepared for Office of Naval Research for the period of Feb. 20, 2010-May 19, 2010, 34 pages.
Verma et al., “Tribological Behavior of Deagglomerated Active Inorganic Nanoparticles for Advanced Lubrication”, Tribology Transactions. Sep. 1, 2008. 51: 673-678.
Adhvaryu, Dr. Antanu, “Multi-component Nanoparticle Based Lubricant Additive to Improve Efficiency and Durability in Engines”, Caterpillar Inc Aug. 7, 2008, 27 pages.
Verma, Arpana, “Fundamental Understanding of the Synthesis and Tribological Behavior of Organic-Inorganic Nanoparticles”, Dec. 2008, University of Arkansas, 147 pages.
Berdinsky et al., “Synthesis of MoS2 nanostruotures from namo-size powder by thermal annealing”, Electron Devices and Materials (2000): EDM (2000) Sibenan Russian Student Workshops on Sep. 19-21, 2000 Piscataway, NJ, USA, pp. 20-28.
Cizaire et al., “Mechanisms of ultra-low friction by hollow inorganic fullerene-like MoS2 nanoparticles”, Surface and Coatings Technology (2002) 160(2-3): pp. 282-287.
Huang et al., “Friction and wear properties of IF-M0S2 as additive in Paraffin oil,” Tribology Letters, vol. 20, Nos. 5-4. Dec. 2005, pp. 247-250.
Rapoport et al., “Fullerene-like WS2 nanopatdes: superior lubricants for harsh conditions”, Advanced Materials, Apr. 17, 2003, vol. 15. Nos. 7-8, pp. 651-655.
Hu, Xianguo, “On the size effect of molybdenum disulfide particles on tribological performance”, Industrial Lubrication and Tribology, 2005, vol. 57, Issue 6, pp. 255-259.
Gustavsoon et al., Nanparticle based and sputtered WS2 low-friction coatings—Differences and similarites with respect to friction mechanisms and tribofilm formulation, Surface & Coating Technol., vol. 232, pp. 616-626, Oct. 15, 2013.
JP Patent Office, Office Action dated May 25, 2015, JP Patent Appln No. 2014-095260 (with English Translation).
Related Publications (1)
Number Date Country
20160046886 A1 Feb 2016 US
Provisional Applications (1)
Number Date Country
60758307 Jan 2006 US
Continuations (2)
Number Date Country
Parent 13921640 Jun 2013 US
Child 14844797 US
Parent 12160758 US
Child 13921640 US